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Evaluation of the Pharmacokinetics/Pharmacodynamics and Safety/Tolerability of IN-C005 and IN-A001 in Healthy Caucasians

10. maj 2022 opdateret af: HK inno.N Corporation

A Randomized, Open-label, Multiple Dosing, Cross-over Phase 1 Clinical Trial to Evaluate Pharmacokinetics/Pharmacodynamics and Safety/Tolerability of IN-C005 and IN-A001 After Oral Administration in Healthy Caucasian Subjects

The purpose of this study is to evaluate pharmacokinetics/pharmacodynamics and safety/tolerability of IN-C005 and IN-A001 after oral administration in healthy Caucasian subjects.

Studieoversigt

Detaljeret beskrivelse

[Part 1] To evaluate the pharmacokinetic (PK)/pharmacodynamic (PD) profiles and safety/tolerability of 100 mg IN-C005 versus 100 mg IN-A001 after multiple oral dosing in healthy Caucasian subjects

[Part 2] To evaluate the PK/PD profiles and safety/tolerability of 50 mg IN-C005 versus 75 mg IN-C005 after multiple oral dosing in healthy Caucasian subjects

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

20

Fase

  • Fase 1

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

      • Seoul, Korea, Republikken, 03080
        • Seoul National University Hopsital
    • Jongro Gu
      • Seoul, Jongro Gu, Korea, Republikken, 03080
        • Seoul National University Hospital

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

19 år til 50 år (Voksen)

Tager imod sunde frivillige

Ja

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  1. Is healthy Caucasian adult aged 19 to 50 years (inclusive) at the time of signing the informed consent form (ICF) (A Caucasian is defined as a European who was born in Europe, has the duration of residence outside of Europe less than 10 years, and both of whose parents and grandparents are European-born).
  2. Has ≥ 18.0 and ≤ 30.0 kg/m2 of body mass index (BMI) with a body weight (BW) ≥ 55.0 kg at screening.
  3. Has a negative result in serum Helicobacter pylori IgG antibody test.
  4. Decides to participate voluntarily in the study after being fully informed of and understanding the study completely, and provides his/her written informed consent prior to screening procedure.
  5. Is eligible for this study in the opinion of the investigator based on the results of physical examination, clinical laboratory tests, interview, etc.

Exclusion Criteria:

  1. Has a history or current evidence of clinically significant disorder of hepatic, renal, nervous, respiratory, endocrine, hemato-oncologic, cardiovascular, urinary, and/or psychiatric system.
  2. Has a history or current evidence of gastrointestinal disease that may affect the safety and PD assessments for study treatment (e.g., gastrointestinal ulcer, gastritis, gastric cramp, gastroesophageal reflux disease, and Crohn's disease) or a history of gastrointestinal surgery (except for simple appendectomy or herniotomy).
  3. Has a history or current evidence of clinically significant hypersensitivity to study drugs or any ingredient of proton pump inhibitors and other drugs (such as aspirin and antibiotics).
  4. Has a positive result on serology tests (for hepatitis B, human immunodeficiency virus [HIV], and hepatitis C).
  5. Has a blood level of total bilirubin, AST (GOT), or ALT (GPT) > 1.5 X upper limit of normal (ULN) based on screening procedures including repeated ones.
  6. Has a calculated eGFR per MDRD equation < 60 mL/min/1.73 m2 based on screening procedures including repeated ones.
  7. Has systolic blood pressure (SBP) of < 90 mmHg or > 140 mmHg, diastolic blood pressure (DBP) of < 50 mmHg or > 95 mmHg, or pulse rate (PR) of < 45 beats/min or > 100 beats/min on vital signs as measured in sitting position after taking a rest for at least 5 minutes at screening.
  8. Has an anatomical disorder that precludes insertion and maintenance of intragastric pH meter catheter or is expected to be intolerable to insertion of intragastric pH meter catheter.
  9. Has a history of drug abuse or has a positive response to drug abuse on urine drug screening test.
  10. Has received any prescription drug or herbal medication within 2 weeks of or any over-the-counter (OTC) drug, dietary supplements, or vitamins within 1 week of scheduled first dose or is expected to receive such medication during the study (Note: a subject may participate in the study at the discretion of the investigator provided the subject meets all the other criteria).
  11. Has participated and received an investigational agent in another clinical trial or bioequivalence study within 6 months prior to the first dose of study treatment (Note: This is not applied to participation in another part of this study).
  12. Has donated whole blood within 2 months prior to the scheduled first dose, or has donated blood components or received transfusion within a month prior to the scheduled first dose.
  13. Has excessive caffeine intake (> 5 units/day), continues the use of alcohol (> 21 units/week, 1 unit = 10 g of pure alcohol), or is unable to stop drinking during hospitalization period.
  14. Has a positive result for cotinine on urine drug screening test or is unable to stop smoking throughout the study.
  15. Is unable to avoid grapefruit-containing foods during the time from 24 hours (hrs) before hospitalization to discharge in Period 1 and Period 2, respectively.
  16. Is unable to avoid caffeine-containing foods (e.g., coffee, tea [red tea, green tee, etc.], soda, coffee milk, and nutritive tonic drink) during the time from 24 hrs before hospitalization to discharge Period 1 and Period 2, respectively.
  17. For all women of childbearing potential (WOCBP) excluding those on amenorrhea for at least 12 months and those who underwent surgical sterilization (bilateral tubal ligation, bilateral oophorectomy, or hysterectomy), has a positive result for pregnancy test (urine hCG) performed prior to the first dose of study treatment or is pregnant or breastfeeding.
  18. Is unable to use a medically acceptable contraceptive method throughout the study. Medically acceptable contraceptive methods include:

    • Use of an intrauterine device with a proven birth control failure rate by the subject or subject's spouse (or partner)
    • Use of (male or female) barrier method with spermicide
    • Surgical sterilization (vasectomy, salpingectomy, tubal ligation, hysterectomy) of the subject or subject's spouse (or partner)
  19. Is determined ineligible for study participation by the investigator for other reasons such as clinical laboratory abnormalities.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Crossover opgave
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Treatment AB
Participants will be randomized to receive IN-C005 Y mg (Treatment A) and IN-A001 Y mg (Treatment B) sequentially in a two-period sequence. There will be a washout period of at least 14 days between Period 1 and Period 2.
Oral tablet
Oral capsule
Eksperimentel: Treatment BA
Participants will be randomized to receive IN-A001 Y mg and IN-C005 Y mg sequentially in a two-period sequence. There will be a washout period of at least 14 days between Period 1 and Period 2.
Oral tablet
Oral capsule
Eksperimentel: Treatment CD
Participants will be randomized to receive IN-C005 Z mg (Treatment C) and IN-C005 X mg (Treatment D) sequentially in a two-period sequence. There will be a washout period of at least 14 days between Period 1 and Period 2.
Oral capsule
Oral capsule
Eksperimentel: Treatment DC
Participants will be randomized to receive IN-C005 X mg and IN-C005 Z mg sequentially in a two-period sequence. There will be a washout period of at least 14 days between Period 1 and Period 2.
Oral capsule
Oral capsule

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Cmax
Tidsramme: Day 1, Day 22
PK: Maximum concentration of drug in plasma
Day 1, Day 22
AUClast
Tidsramme: Day 1, Day 22
PK: Area under the plasma drug concentration-time curve from 0 to last point of measurable concentration
Day 1, Day 22
Cmax,ss
Tidsramme: Day 7 and Day 28
PK: Maximum (peak) steady-state plasma drug concentration during a dosage interval
Day 7 and Day 28
AUCtau,ss
Tidsramme: Day 7 and Day 28
PK: Area under the plasma drug concentration-time curve for a dosing interval at steady state
Day 7 and Day 28
Percent duration of pH ≥4 in 24 hrs (duration %)
Tidsramme: Day 1, Day 22
PD: pH parameter
Day 1, Day 22
Percent duration of pH ≥4 in 24 hrs (duration %)
Tidsramme: Day 7, Day 28
PD: pH parameter
Day 7, Day 28
Change from baseline in percent duration of pH ≥4 in 24 hrs
Tidsramme: Day 1, Day 7, Day 22, Day 28
PD: pH parameter
Day 1, Day 7, Day 22, Day 28

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
AUCinf
Tidsramme: Day 1, Day 22
PK: Area under the plasma drug concentration-time curve from time 0 to infinity
Day 1, Day 22
Tmax
Tidsramme: Day 1, Day 22
PK: The time of peak concentration
Day 1, Day 22
t1/2
Tidsramme: Day 1, Day 22
PK: Terminal half-life
Day 1, Day 22
CL/F
Tidsramme: Day 1, Day 22
PK: Apparent Clearance
Day 1, Day 22
Vd/F
Tidsramme: Day 1, Day 22
PK: Apparent volume of distribution after extravascular administration
Day 1, Day 22
Tmax,ss
Tidsramme: Day 7, Day 28
PK: Time to reach Cmax
Day 7, Day 28
t1/2,ss
Tidsramme: Day 7, Day 28
PK: Apparent first order terminal elimination half-life
Day 7, Day 28
Cmin,ss
Tidsramme: Day 7, Day 28
PK: Minimum observed non zero concentration between dose time and dose time + dosing interval, tau
Day 7, Day 28
Cavg,ss
Tidsramme: Day 7, Day 28
PK: The average concentration at steady state, calculated as the ratio of AUCtau to the dosing interval, tau
Day 7, Day 28
CLss/F
Tidsramme: Day 7, Day 28
PK: The total body clearance at steady state after oral administration
Day 7, Day 28
Vd,ss/F
Tidsramme: Day 7, Day 28
PK: Apparent volume of distribution after extravascular administration in steady state
Day 7, Day 28
PTF
Tidsramme: Day 7, Day 28
PK: Peak to trough fluctuation
Day 7, Day 28
R
Tidsramme: Day 7, Day 28
PK: Accumulation ratio
Day 7, Day 28
Percent duration of pH ≥3 in 24 hrs
Tidsramme: Day 1, Day 7, Day 22, Day 28
PD: pH parameter
Day 1, Day 7, Day 22, Day 28
Change from baseline in percent duration of pH ≥3 in 24 hrs
Tidsramme: Day 1, Day 7, Day 22, Day 28
PD: pH parameter
Day 1, Day 7, Day 22, Day 28
Percent duration of pH ≥6 in 24 hrs
Tidsramme: Day 1, Day 7, Day 22, Day 28
PD: pH parameter
Day 1, Day 7, Day 22, Day 28
Change from baseline in percent duration of pH ≥6 in 24 hrs
Tidsramme: Day 1, Day 7, Day 22, Day 28
PD: pH parameter
Day 1, Day 7, Day 22, Day 28
Mean and median pH in 24 hrs
Tidsramme: Day 1, Day 7, Day 22, Day 28
PD: pH parameter
Day 1, Day 7, Day 22, Day 28
Change from baseline in mean pH in 24 hrs
Tidsramme: Day 1, Day 7, Day 22, Day 28
PD: pH parameter
Day 1, Day 7, Day 22, Day 28
Change from baseline in median pH in 24 hrs
Tidsramme: Day 1, Day 7, Day 22, Day 28
PD: pH parameter
Day 1, Day 7, Day 22, Day 28
AUEGlast
Tidsramme: Day 1, Day 7, Day 22, Day 28
PD(Gastrin): Area under the concentration-time curve of Serum Gastrin from 0 to last point of quantifiable concentration
Day 1, Day 7, Day 22, Day 28
Gmax
Tidsramme: Day 1, Day 7, Day 22, Day 28
Gastrin: Maximum gastrin level
Day 1, Day 7, Day 22, Day 28
ΔAUEGlast
Tidsramme: Day 1, Day 7, Day 22, Day 28
PD(Gastrin): Change from baseline in AUEGlast
Day 1, Day 7, Day 22, Day 28
ΔGmax
Tidsramme: Day 1, Day 7, Day 22, Day 28
PD(Gastrin): Change from baseline in Gmax
Day 1, Day 7, Day 22, Day 28

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Efterforskere

  • Ledende efterforsker: In-Jin Jang, MD, Ph.D, Clinical Pharmacology and Therapeutics, Seoul National University Hospital

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

6. september 2021

Primær færdiggørelse (Faktiske)

18. november 2021

Studieafslutning (Faktiske)

30. november 2021

Datoer for studieregistrering

Først indsendt

5. juli 2021

Først indsendt, der opfyldte QC-kriterier

6. august 2021

Først opslået (Faktiske)

13. august 2021

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

16. maj 2022

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

10. maj 2022

Sidst verificeret

1. august 2021

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • IN_BTK_102

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

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Kliniske forsøg med IN-A001 Y mg

3
Abonner